Evidence map›Paper›PMID 38919077›Full record

ArticleCurrent pharmaceutical design2024

Design, Synthesis and Evaluation of a Novel Teoptinib Derivative as an Effective Anti-hepatocellular Carcinoma Agent.

Huijuan Yu, Xiaodong Zhang, Jiayu Li, Kaimei Wang, Changjun Yin, Xinshu Li, Lianyun Li, Guang Shao, Shaowen Jin

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Article in Current pharmaceutical design, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Huijuan YuGuangdong Key Laboratory of Animal Conservation and Resource Utilization, Institute of Zoology, Guangdong Academy of Sciences, Guangzhou 510275, China.
Xiaodong ZhangSchool of Chemistry, Sun Yat-Sen University, Guangzhou 510275, China.
Jiayu LiGuangdong Key Laboratory of Animal Conservation and Resource Utilization, Institute of Zoology, Guangdong Academy of Sciences, Guangzhou 510275, China.
Kaimei WangDepartment of Pediatrics, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou 510120, China.
Changjun YinDepartment of Gastrointestinal Surgery, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou 510120, China.
Xinshu LiSchool of Chemistry, Sun Yat-Sen University, Guangzhou 510275, China.
Lianyun LiSchool of Chemistry, Sun Yat-Sen University, Guangzhou 510275, China.
Guang ShaoSchool of Chemistry, Sun Yat-Sen University, Guangzhou 510275, China.
Shaowen JinDepartment of Gastrointestinal Surgery, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou 510120, China.

Funding

National Natural Science Foundation of China (NSFC) 81602125,82104228
6 · The paper itself

Abstract

BACKGROUND & PURPOSE: Hepatocellular Carcinoma (HCC) is a type of liver cancer known for its poor prognosis and high mortality. Teoptinib is a highly selective MET inhibitor that has been used in the treatment of liver cancer. Although good progress has been made in clinical treatment, further improvement is still needed. In this study, a series of novel Teoptinib derivatives were synthesized and evaluated as anti-cancer agents for the treatment of liver cancer, and an oral nanodrug delivery system was also explored.

methodsA series of novel Teoptinib derivatives were synthesized, and an oral nanodrug delivery system was also explored. HPLC, high-resolution mass spectrometer and NMR were used to determine the structure and molecular formula of the synthesized compounds. Zeta potential assay was used to access the particle size distribution and zeta potential of the nanoparticles. MTT assay, cell colony formation assay, cell apoptosis inhibition assay, cell scratch assay, and the MHCC-97H xenograft model of nude mice assay were used to evaluate the

resultsCompound (R)-10 showed the best antitumor activity with 0.010 μM of the IC50 value against MHCC-97H, a human liver cancer cell line with high c-Met expression. The MHCC-97H xenograft model of nude mice assay showed that nano-prodrug of compound (R)-10 exhibited good in vivo activity with 87.67% of the TGI at the dosage of 8 mg/kg.

conclusionWe designed and synthesized a series of c-Met inhibitors containing different side chains and chiral centers as anti-liver cancer agents. Among them, compound (R)-10 shows a promising effect as a lead molecule for further study in the treatment of liver cancer. The successful incorporation of (R)-10 into a novel oral nanodrug delivery system highlights the importance of effective drug delivery systems for enhanced therapeutic efficacy.

Indexed as

Antineoplastic AgentsApoptosisCarcinoma, HepatocellularCell ProliferationDrug DesignLiver NeoplasmsMice, NudeAnimalsCell Line, TumorDose-Response Relationship, DrugDrug Screening Assays, AntitumorHumansLiver Neoplasms, ExperimentalMiceMice, Inbred BALB CMolecular StructureAntineoplastic AgentsProto-Oncogene Proteins c-metanti-liver cancer agents.chiral synthesisc-Met inhibitorhepatocellular carcinomanano-prodrugNovel teoptinib derivatives

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.